p.Arg38 Ala49del variant of SOCS1 (O15524)
p.Arg38 Ala49del in SOCS1 (O15524) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
p.Arg38 Ala49del variant details
- rs1239337863
- gnomAD 16-11255335-CGGGG
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.222
- CADD 19.90
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available